RESPIRATORY BLOCK PATHOLOGY L4

1. RESPIRATORY BLOCK PATHOLOGY L4 Pulmonary infection Dr. MahaArafah Feb 2012

2. At the end of this lecture, the student should be able to: A] Understand that pneumonia is an inflammatory condition of the lung characterized by consolidation (solidification) of the pulmonary tissue. B] Is aware of the pathogenesis of pneumonia and its classification which principally include bronchopneumoniae, lobar pneumonia and atypical pneumonia. C] Is able to appreciate the aetiology and pathogenesis of lung abscess.

3. CONTENTS 1] General considerations and clinical characteristics of pneumonia.  2] Morphologic types of pneumonias including: a. lobar pneumonia b. bronchopneumonia c. interstitial pneumonia (atypical pneumonia) with special emphasis on mycoplasma pneumonia, viral pneumonia and ornithosis (Chlamydia induced). 3] Pneumocystiscarinii pneumonia as the most common opportunistic infection in patients with AIDS.  4] Hospital acquired gram negative pneumonias.  5] Lung abscess: causes and manifestations.

4. Pulmonary infections (Pneumonia) Pneumonia can be very broadly defined as any infection in the lung

5. Pulmonary infections • Respiratory tract infections are more frequent than infections of any other organ and account for the largest number of workdays lost in the general population, why? • The epithelium of the lung is exposed to liters of contaminated air • Nasopharyngeal flora are aspirated during sleep • Underlying lung diseases render the lung parenchyma vulnerable to virulent organism.

6. Pathogenesis of pneumonia Each day, the respiratory tract is exposed to more than 10,000 liters of air containing hazardous dust, Chemicals and microorganisms. • Particle > 10 mm deposited in nose. • Particle 3-10 mm impacted in trachea and bronchi. • Particle 1-3 mm (bacteria) deposited in terminal airways and alveoli. • Smaller particles < 1 mm may remain suspended in air. • Normal lung is free from bacteria.

7. Pathogenesis of pneumonia • Pneumoniacan result whenever: • defense mechanisms are impaired • the resistance of the host in general is lowered.

8. Pulmonary host defenses • Upper airways: • Nasopharynx: • Oropharynx Nasal hair, turbinates, mucociliary apparatus, IgA secretion • Saliva, sloughing of epithelium, local complement production, interference from resident flora

9. Pulmonary host defenses • Upper airways: • Conducting airways (trachea and bronchi): • Cough, epiglottic reflexes, sharp angled branches of the airways, mucociliary apparatus, Immunoglobulin (IgM, IgG, and IgA) secretion

10. Pulmonary host defenses • Upper airways: • Conducting airways(trachea and bronchi): • Lower respiratory tract: • Alveolar lining fluid ( surfactant, immunoglobulin, complement and fibronectin), Cytokines (IL-1, TNF), alveolar macrophages, polymorphonuclear leukocyte, cell mediated immunity

11. Pathogenesis of pneumonia Impaired defense mechanisms: • Loss or suppression of the cough reflex, as a result of coma, anesthesia, neuromuscular disorders, drugs, or chest pain. • Injury to the mucociliary apparatus, by either impairment of ciliary function or destruction of ciliated epithelium e.g. cigarette smoke, inhalation of hot or corrosive gases, viral diseases, or genetic disturbances • Interference with the phagocytic or bactericidal action of alveolar macrophages by alcohol, tobacco smoke, anoxia, or oxygen intoxication • Pulmonary congestion and edema • Accumulation of secretions e.g. cystic fibrosis and bronchial obstruction • Defect in innate immunity Include neutrophil, complement, humoral and cell mediated immune defects

12. Pathogenesis of pneumonia • General factors that affect resistance: • chronic diseases • immunologic deficiency • treatment with immunosuppressive agents • leukopenia • unusually virulent infections.

13. Pathogenesis of pneumonia • One type of pneumonia sometimes predisposes to another, especially in debilitated patients. • Portal of entry for most pneumonias is the respiratory tract, hematogenous spread from one organ to other organs can occur. • Many patients with chronic diseases acquire terminal pneumonias while hospitalized (nosocomial infection).

14. Pathology of Pneumonia • Pneumonia can be acute or chronic • The histologic spectrum may vary: • Fibrinopurulent alveolar exudate • Mononuclear interstitial infiltrate • Granulomatous inflammation Pneumonia Atypical Pneumonia e.g. Tuberculosis

15. The pneumonia syndromes • Community-Acquired Acute Pneumonia • Community-Acquired Atypical Pneumonia • Nosocomial Pneumonia • Aspiration Pneumonia • Chronic Pneumonia • Pneumonia in the Immunocompromised Host

16. Bacterial Pneumonia • Bacterial invasion of lung parenchyma evoke exudation of fibrinpurulent fluid in the alveoli and solidification. • Classification may be made according to causative agent or gross anatomic distribution of the disease.

17. Anatomic distribution of pneumonia • Bronchopneumonia: -Represent an extension from preexisting bronchitis or bronchiolitis. -Extremely common tends to occur in two extremes of life. • Lobar pneumonia: - Acute bacterial infection of a large portion of a lobe or entire lobe. -Classic lobar pneumonia is now infrequent.

18. Bronchopneumonia • – most common agents are: • Streptococcus pneumonea, • Haemophilus Influenza, • Pseudomonas Aeroginosa • coliform bacteria. • Lobar pneumonia • - 90-95% are caused by pneumococci • (type 1,3,7 & 2) • - Rare agents: K. pneumoniae • staphylococci - streptococci • H. influenzae - Pseudomonas and Proteus

19. Overlap of the two patterns often occur. • Identification of clinical pattern is more important.

20. The pneumonia syndromes • Community-Acquired Acute Pneumonia • Community-Acquired Atypical Pneumonia • Nosocomial Pneumonia • Aspiration Pneumonia • Chronic Pneumonia • Pneumonia in the Immunocompromised Host

21. Etiology of pneumonia Community-Acquired Acute Pneumonia • Bacterial • Can follows viral URT infection • Sudden onset of high fever, chills, pleuritic chest pain and productive cough, may be with hemoptysis • Streptococcus pneumoniaeis the most common cause of Community-Acquired Acute Pneumonia • Frequently affected pt. are those with: • Underlying chronic disease e.g. DM, COPD, and CHF • Congenital or acquired immune deficiency • Decreased or absent splenic function • Other causative organisms are: • Haemophilusinfluenzae, Moraxellacatarrhalis, Staphylococcus aureus, Legionellapneumophila, Enterobacteriaceae (Klebsiellapneumoniae) and Pseudomonas spp. S. aureus lung: abscess and empyema • P. aeruginosa is most commonly seen in nosocomial pneumonia, is associated with infections in cystic fibrosis

22. Morphology of pneumoniaCommunity-Acquired Acute Pneumonia • Lobar or bronchopneumonia may occur. • The lower lobes or the right middle lobe are most frequently involved. • Widespread fibrinosuppurative consolidation.

23. Community-Acquired Acute Pneumonia Stages of pneumonia • Congestion – lobes are heavy, red and boggy; histologically, vascular congestion can be seen with proteinaceous fluid, scattered neutrophils and many bacteria in the alveoli. • Red hepatization – alveolar spaces are packed with neutrophils, red cells, and fibrin, pleura – fibrinous or fibrinopurulent exudate. • Gray hepatization – lung is dry, gray and firm and the fibrinous exudate persists within the alveoli. • Resolution – exudates within the alveoli are enzymatically digested.

24. Community-Acquired Acute Pneumonia Morphology of pneumonia Congestion – vascular congestion can be seen with proteinaceous fluid, scattered neutrophils and many bacteria in the alveoli. Red hepatization – alveolar spaces are packed with neutrophils, red cells, and fibrin, pleura fibrinous or fibrinopurulentexudate

25. Community-Acquired Acute Pneumonia Stages of pneumonia Gray hepatization – fibrinousexudate persists within the alveoli.

26. Community-Acquired Acute Pneumonia Stages of pneumonia Resolution – exudates within the alveoli are enzymatically digested.

27. Clinical features • Abrupt onset of high fever, shaking chills, and cough productive of mucopurulent sputum; occasional patients may have hemoptysis. • When fibrinosuppurative pleuritis is present, it is accompanied by pleuritic pain and pleural friction rub

28. Complications of pneumonia • Tissue destruction (abscess). • Empyema. • Organization of alveolar exudate – solid fibrinous tissue. • Bacteremic dissemination may lead to meningitis, arthritis or infective endocarditis.

29. Community-Acquired Acute Pneumonia Dx & Rx • Examination of Gram-stained sputum smear is helpful in diagnosis • Blood culture is more specific (only +ve in 20% to 30% of pt.) • Pneumococcal pneumonia respond to penicillin Rx

30. The pneumonia syndromes • Community-Acquired Acute Pneumonia • Community-Acquired Atypical Pneumonia • Nosocomial Pneumonia • Aspiration Pneumonia • Chronic Pneumonia • Pneumonia in the Immunocompromised Host

31. Community-Acquired Atypical Pneumonia:Primary atypical pneumonia • Pt. Usually present with flulike symptoms with pharyngitis evolved into laryngitis, trachiobronchitis and pneumonia with little sputum and no lung consolidation • Mycoplasmapneumoniae, Chlamydia spp. (C. pneumoniae, C. psittaci, C. trachomatis) Inhalation of dried excreta of birds lead to Ornithosis(Psittacosis)due to chlamydia infection • Coxiellaburnetti (Q fever) • Viruses: respiratory syncytial virus, parainfluenza virus (children); influenza A and B (adults); adenovirus and SARS virus (Severe Acute Respiratory Syndrome )

32. Mycoplasma pneumonia • This is the most common form of interstitial pneumonia • it usually occurs in children and young adults and it may occur in epidemics. • Onset is more insidious compared to bacterial pneumonia and usually follows a mild, self-limited course. •  Characteristics include an inflammatory reaction confined to the interstitiium, with no exudate in alveolar spaces and intra-alveolar hyaline membranes. • Diagnosis is by sputum cultures, requiring several weeks of incubation and by complement fixing antibodies. • Mycoplasma pneumonia may be associated with non specific cold agglutinins reactive to red cells. This phenomenon is the basis for a quick and easy laboratory test that can provide early diagnostic information.

33. Community-Acquired Atypical Pneumonia:Primary atypical pneumonia Acute febrile respiratory disease characterized by patchy inflammatory infiltration by lymphocyte and plasma cells largely confined to the alveolar septa and pulmonary interstitium- (Interstitial pneumonitis).

34. The pneumonia syndromes • Community-Acquired Acute Pneumonia • Community-Acquired Atypical Pneumonia • Nosocomial Pneumonia • Aspiration Pneumonia • Chronic Pneumonia • Pneumonia in the Immunocompromised Host

35. Nosocomial pneumonia hospital acquired pneumonia • Common in pt. with sever underlying conditions e.g. immunosuppression, prolonged antibiotic therapy, intravascular catheter and pt. with mechanical ventlator • Organism include: Gram-negative rods belonging to Enterobacteriaceae :Serratiamarcescens, Escherichia coli, Klebsiella spp. , Pseudomonas aeruginosa.

36. The pneumonia syndromes • Community-Acquired Acute Pneumonia • Community-Acquired Atypical Pneumonia • Nosocomial Pneumonia • Aspiration Pneumonia • Chronic Pneumonia • Pneumonia in the Immunocompromised Host

37. Aspiration pneumonia • Aspiration Pneumonia • Occur in debilitated patients or those who aspirated gastric contents • Chemical injury due gastric acid and bacterial infection including: • Anaerobic oral flora (Bacteroides, Prevotella, Fusobacterium, Peptostreptococcus), admixed with aerobic bacteria (Streptococcus pneumoniae, Staphylococcus aureus, Haemophilasinfluenzae, and Pseudomonas aeruginosa • A necrotizing pneumonia with fulminant clinical course, common complication (abscess) and frequent cause of death.

38. The pneumonia syndromes • Community-Acquired Acute Pneumonia • Community-Acquired Atypical Pneumonia • Nosocomial Pneumonia • Aspiration Pneumonia • Chronic Pneumonia • Tuberculosis is by far the most important entity within the spectrum of chronic pneumonias • Pneumonia in the Immunocompromised Host

39. The pneumonia syndromes • Community-Acquired Acute Pneumonia • Community-Acquired Atypical Pneumonia • Nosocomial Pneumonia • Aspiration Pneumonia • Chronic Pneumonia • Pneumonia in the Immunocompromised Host

40. Pneumonia in the Immunocompromised Host • Cytomegalovirus • Pneumocystis jiroveci • Mycobacterium avium-intracellulare • Invasive aspergillosis • Invasive candidiasis • "Usual" bacterial, viral, and fungal organisms

41. Pneumocystis Pneumonia • is the most common opportunistic infection in patients with acquired immunodeficiency syndrome (AIDS); it also occurs in other forms of immunodeficiency. • It is caused by pneumocystiscarinii(recently renamed Pneumocystisjiroveci) which is now classified as a fungus. • Diagnosis is by morphologic demonstration of the organism in biopsy or bronchial washing specimens.

42. Pneumocystis Pneumonia Microscopically, involved areas of the lung demonstrate a characteristic intra-alveolar foamy, pink-staining exudate with H&E stains Silver stain demonstrates cup-shaped cyst walls within the exudate

43. Lung abscess • A localized suppurative process within the pulmonary parenchyma • features: tissue necrosis and marked acute inflammation • Posssile causes: aerobic and anaerobic e.g. streptococci, Staphylococcus aureus, and many gram negative organisms • Can follow aspiration ( one abscess of Rt. lung) • occur as complication of pneumonia ( multiple) • Abscess is filled with necrotic suppurativedebri

44. Chest radiograph of a patient who had fever, cough, foul-smelling and bad-tasting sputum, an almost diagnostic feature of anaerobic lung abscess. a fluid-containing cavity

45. Chest X- ray Change in position evoke paroxysm of cough

46. Lung abscess

47. Lung abscess • Complications • Pleural involvement (empyema) formation resulting from a bronchopleural fistula • massive hemoptysis, spontaneous rupture into uninvolved lung segments • non-resolution of abscess cavity • Bacteremia could result in brain abscess and meningitis • with antibiotic therapy 75% of abscess resolve